{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/skill/electronic-health-records"},"x-facet":{"type":"skill","slug":"electronic-health-records","display":"Electronic Health Records","count":2},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d301fe8d-333"},"title":"Visiting Faculty","description":"<p>Job Description:</p>\n<p>Scale AI invites applications for a Visiting Faculty position with expertise in Machine Learning in the Healthcare Domain. The ideal candidate will have a strong background in Computer Science, Bioinformatics, or a closely related field, and a proven track record of innovative research in Machine Learning and its Applications in Healthcare Domain.</p>\n<p>Responsibilities:</p>\n<p>Develop cutting-edge research programs that align with areas such as utilizing electronic health records and non-clinical data for modeling and predicting health behaviors and outcomes. Collaborate with engineers at Scale AI to engage in collaborative research and development. Address issues of bias and fairness in AI within healthcare.</p>\n<p>Required Qualifications:</p>\n<p>A Ph.D. in Computer Science, Biostatistics, Biomedical Informatics, or a closely related quantitative field. Demonstrated excellence in research with a focus on Machine Learning and NLP applications in Healthcare, evidenced by high-impact publications and/or significant grant funding. Strong communication and collaboration skills.</p>\n<p>Please note that our policy requires a 90-day waiting period before reconsidering candidates for the same role.</p>\n<p>About Us:</p>\n<p>At Scale, our mission is to develop reliable AI systems for the world&#39;s most important decisions.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_d301fe8d-333","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Scale AI","sameAs":"https://scale.com/","logo":"https://logos.yubhub.co/scale.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/scaleai/jobs/4623605005","x-work-arrangement":"remote","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Machine Learning","NLP","Electronic Health Records","Non-Clinical Data","Bias and Fairness in AI"],"x-skills-preferred":[],"datePosted":"2026-04-18T15:36:50.499Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"United States"}},"jobLocationType":"TELECOMMUTE","employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Machine Learning, NLP, Electronic Health Records, Non-Clinical Data, Bias and Fairness in AI"},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d67b1b38-d42"},"title":"Research Phlebotomist","description":"<p>Meet knownwell, a weight-inclusive healthcare company that is changing the way obesity care is delivered. We offer weight management, primary care, nutrition counseling, and health coaching. Our care model combines in-clinic and virtual care to bring support to patients where and when they need it.</p>\n<p>The Research Phlebotomist plays a vital hands-on role in the execution of clinical trials, serving as a key point of contact for study participants throughout their research journey. Working under the direction of the Clinical Research Coordinator and/or Clinical Research Manager, the Research Phlebotomist is primarily responsible for patient-facing activities, including study visits, specimen collection and processing, data entry, and clinical assessments.</p>\n<p><strong>Responsibilities</strong></p>\n<p>Patient Interaction &amp; Visit Support</p>\n<ul>\n<li>Serve as a primary point of contact for study participants during on-site visits, providing a welcoming and professional experience.</li>\n<li>Guide participants through study visit procedures, answering questions and ensuring they feel informed and comfortable throughout the process.</li>\n<li>Assist in the informed consent process, ensuring participants understand study expectations, risks, and benefits prior to enrollment.</li>\n<li>Monitor and document participant well-being during visits, escalating any safety concerns to the supervising Coordinator or Investigator promptly.</li>\n<li>Schedule and confirm participant appointments, sending reminders and managing visit logistics to support timely enrollment and retention.</li>\n</ul>\n<p>Clinical Assessments</p>\n<ul>\n<li>Perform and document vital signs, including blood pressure, heart rate, temperature, respiratory rate, and weight.</li>\n<li>Conduct electrocardiograms (EKGs) per protocol, ensuring proper lead placement and tracing quality.</li>\n<li>Perform phlebotomy (blood draws) in accordance with study protocols and applicable safety standards.</li>\n<li>Administer and document other protocol-specified assessments as trained and permitted by scope of practice.</li>\n</ul>\n<p>Specimen Collection &amp; Processing</p>\n<ul>\n<li>Collect, process, label, and store biological samples (blood, urine, etc.) per study protocol and applicable regulatory requirements.</li>\n<li>Ensure proper cold-chain handling and timely shipment of samples to central labs or sponsors.</li>\n<li>Maintain specimen logs and chain-of-custody documentation accurately.</li>\n<li>Ensure proper disposal of biohazardous materials in compliance with institutional and regulatory standards.</li>\n</ul>\n<p>Data Entry &amp; Documentation</p>\n<ul>\n<li>Accurately enter study data into the clinical trial management system (CTMS) and/or electronic data capture (EDC) systems in a timely manner.</li>\n<li>Complete and maintain source documentation for all participant visits, assessments, and clinical activities.</li>\n<li>Perform basic quality control checks on data entry to ensure accuracy and completeness.</li>\n<li>Flag discrepancies or missing data to the supervising Coordinator for resolution.</li>\n</ul>\n<p>Site &amp; 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